4-Phenylphenol - analytical standard,for environmental analysis, high purity , CAS No.92-69-3

Item Number
P100425
Grouped product items
SKUSizeAvailabilityPrice Qty
P100425-250mg
250mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$102.90

Basic Description

Synonyms4-Biphenylol | AI3-00080 | AMY40490 | HMS1369I22 | para-Hydroxydiphenyl | Phenol p-phenyl | AB01331816-02 | Phenol, p-phenyl | p-phenyl phenol | DTXSID7021152 | DTXCID601152 | NCGC00249191-01 | NCGC00256447-01 | (1,1'-Biphenyl)-4-ol | 1-Hydroxy-4-phenylbe
Specifications & Purityanalytical standard, for environmental analysis
Shipped InNormal
Gradeanalytical standard, for environmental analysis
Product Description

4-Phenylphenol (4-hydroxybiphenyl, 4-HBP), a biaryl compound, is a weakly acidic 4-arylphenol. A study on its crystalline structure has been reported. Its rapid, green synthesis via a Pd(0)-catalyzed Suzuki cross-coupling reaction in water has been reported. The standard molar enthalpy of formation of 4-phenylphenol has been evaluated using combustion calorimetry. The solid-matrix luminescence properties for 4-phenylphenol adsorbed on filter paper has been investigated.A study conducted using the yeast two-hybrid assay suggests that it shows estrogenic activity

Associated Targets(Human)

ESR2 Tclin Estrogen receptor beta (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PTPN1 Tchem Tyrosine-protein phosphatase non-receptor type 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SULT1A1 Tchem Sulfotransferase 1A1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
UGT2B7 Tchem UDP-glucuronosyltransferase 2B7 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
UGT2B10 Tbio UDP-glucuronosyltransferase 2B10 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
UGT2B15 Tbio UDP-glucuronosyltransferase 2B15 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
UGT2B28 Tbio UDP-glucuronosyltransferase 2B28 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
UGT1A10 Tbio UDP-glucuronosyltransferase 1-10 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
UGT1A1 Tchem UDP-glucuronosyltransferase 1-1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
UGT1A4 Tbio UDP-glucuronosyltransferase 1-4 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
UGT1A8 Tbio UDP-glucuronosyltransferase 1-8 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
UGT1A9 Tbio UDP-glucuronosyltransferase 1-9 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TTR Tclin Transthyretin (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
BCL2L1 Tchem Bcl-2-like protein 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
VEGFA Tclin Vascular endothelial growth factor A (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ALB Tchem Serum albumin (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
AR Tclin Androgen receptor (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
UGT1A3 Tbio UDP-glucuronosyltransferase 1-3 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
UGT1A6 Tbio UDP-glucuronosyltransferase 1-6 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
UGT1A7 Tbio UDP-glucuronosyltransferase 1-7 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
UGT2A1 Tbio UDP-glucuronosyltransferase 2A1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
UGT2B4 Tbio UDP-glucuronosyltransferase 2B4 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
UGT2B17 Tbio UDP-glucuronosyltransferase 2B17 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
MMP3 Tchem Stromelysin-1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
VEGFA Tclin Vascular endothelial growth factor A (159 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALB Tchem Serum albumin (2651 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MMP3 Tchem Matrix metalloproteinase 3 (3433 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A4 Tbio UDP-glucuronosyltransferase 1A4 (288 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-29 (80576 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
U-251 (51189 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
U-87 MG (3946 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCL2L1 Tchem Apoptosis regulator Bcl-X (2604 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT2B7 Tchem UDP-glucuronosyltransferase 2B7 (787 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT2B17 Tbio UDP-glucuronosyltransferase 2B17 (197 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT2B4 Tbio UDP-glucuronosyltransferase 2B4 (139 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT2B10 Tbio UDP-glucuronosyltransferase 2B10 (42 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT2B15 Tbio UDP-glucuronosyltransferase 2B15 (172 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT2B28 Tbio UDP-glucuronosyltransferase 2B28 (9 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A1 Tchem UDP-glucuronosyltransferase 1-1 (448 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A6 Tbio UDP-glucuronosyltransferase 1-6 (221 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A7 Tbio UDP-glucuronosyltransferase 1-7 (106 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A8 Tbio UDP-glucuronosyltransferase 1-8 (233 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A9 Tbio UDP-glucuronosyltransferase 1-9 (343 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A10 Tbio UDP-glucuronosyltransferase 1-10 (257 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT2A1 UDP-glucuronosyltransferase 2A1 (59 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Sult1a1 Aryl sulfotransferase (136 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ttr Transthyretin (14 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ptpn1 Protein-tyrosine phosphatase 1B (270 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bacillus subtilis (32866 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Human papillomavirus (81 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR1 Estrogen receptor (4 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name 4-phenylphenol
INCHI InChI=1S/C12H10O/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9,13H
InChi Key YXVFYQXJAXKLAK-UHFFFAOYSA-N
Canonical SMILES C1=CC=C(C=C1)C2=CC=C(C=C2)O
Isomeric SMILES C1=CC=C(C=C1)C2=CC=C(C=C2)O
WGK Germany 2
RTECS DV5850000
PubChem CID 7103
UN Number 2430
Molecular Weight 170.21
Beilstein 1907452

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

Find and download the COA for your product by matching the lot number on the packaging.

1 results found

Lot NumberCertificate TypeDateItem
C1628152Certificate of AnalysisOct 10, 2023 P100425

Chemical and Physical Properties

SolubilitySoluble in water (0.7 mg/ml at 20°C), ether, most common organic solvents, methanol, and chloroform.
Flash Point(°F)165℃
Flash Point(°C)165℃
Boil Point(°C)321°C
Melt Point(°C)164-166°C

Safety and Hazards(GHS)

Pictogram(s) GHS09,   GHS07
Signal Warning
Hazard Statements

H315:Causes skin irritation

H411:Toxic to aquatic life with long lasting effects

H317:May cause an allergic skin reaction

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P273:Avoid release to the environment.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P272:Contaminated work clothing should not be allowed out of the workplace.

P333+P313:IF SKIN irritation or rash occurs: Get medical advice/attention.

P362+P364:Take off contaminated clothing and wash it before reuse.

P391:Collect spillage.

P332+P317:If skin irritation occurs: Get medical help.

WGK Germany 2
RTECS DV5850000
Merck Index 7305

Related Documents

Citations of This Product

1. Li-Ying Bo, Zhi-Qin Pan, Tian-Ying Sun, Guo-Jun Du, Duo Zhang, Zhi-Qiang Song, Chun-Li Song, Ren Jian.  (2023)  Effect of Carrot Juice on the Texture Properties, Rheology, and Microstructure of Yoghurt.  JOURNAL OF FOOD QUALITY,  2023  (9971055).  [PMID:] [10.1155/2023/9971055]
2. Yao Ma, Jinfan Chen, Xiaodong Du, Chunsheng Xie, Jiangmin Zhou, Xueqin Tao, Zhi Dang, Guining Lu.  (2023)  Efficient removal of polybrominated diphenyl ethers from soil washing effluent by dummy molecular imprinted adsorbents: Selectivity and mechanisms.  Journal of Environmental Sciences,  129  (45).  [PMID:36804241] [10.1016/j.jes.2022.08.026]
3. Yamin Xiong, Lihong Zhou, Xiaoxia Peng, Huiling Li, Hui Wang, Leiliang He, Peili Huang.  (2020)  A specific short peptide-assisted enhanced chemiluminescence resonance energy transfer (CRET) for label-free and ratiometric detection of copper ions in complex samples.  SENSORS AND ACTUATORS B-CHEMICAL,  320  (128411).  [PMID:] [10.1016/j.snb.2020.128411]
4. Jian Wang, Peiping Zhang, Congcong Wang, Xuda Zheng, Yuanjun Zhao, Lina Li, Shiding Miao.  (2020)  Band structure tunable synthesis of photocatalytic porous aromatic frameworks via Scholl reaction.  MATERIALS & DESIGN,  186  (108371).  [PMID:] [10.1016/j.matdes.2019.108371]
5. Qian Geng,Xin-Huai Zhao.  (2015-09-08)  Influences of exogenous probiotics and tea polyphenols on the production of three acids during the simulated colonic fermentation of maize resistant starch..  Journal of food science and technology,  52  ((9)): (5874-5881).  [PMID:26345003]

References

1. Li-Ying Bo, Zhi-Qin Pan, Tian-Ying Sun, Guo-Jun Du, Duo Zhang, Zhi-Qiang Song, Chun-Li Song, Ren Jian.  (2023)  Effect of Carrot Juice on the Texture Properties, Rheology, and Microstructure of Yoghurt.  JOURNAL OF FOOD QUALITY,  2023  (9971055).  [PMID:] [10.1155/2023/9971055]
2. Yao Ma, Jinfan Chen, Xiaodong Du, Chunsheng Xie, Jiangmin Zhou, Xueqin Tao, Zhi Dang, Guining Lu.  (2023)  Efficient removal of polybrominated diphenyl ethers from soil washing effluent by dummy molecular imprinted adsorbents: Selectivity and mechanisms.  Journal of Environmental Sciences,  129  (45).  [PMID:36804241] [10.1016/j.jes.2022.08.026]
3. Yamin Xiong, Lihong Zhou, Xiaoxia Peng, Huiling Li, Hui Wang, Leiliang He, Peili Huang.  (2020)  A specific short peptide-assisted enhanced chemiluminescence resonance energy transfer (CRET) for label-free and ratiometric detection of copper ions in complex samples.  SENSORS AND ACTUATORS B-CHEMICAL,  320  (128411).  [PMID:] [10.1016/j.snb.2020.128411]
4. Jian Wang, Peiping Zhang, Congcong Wang, Xuda Zheng, Yuanjun Zhao, Lina Li, Shiding Miao.  (2020)  Band structure tunable synthesis of photocatalytic porous aromatic frameworks via Scholl reaction.  MATERIALS & DESIGN,  186  (108371).  [PMID:] [10.1016/j.matdes.2019.108371]
5. Qian Geng,Xin-Huai Zhao.  (2015-09-08)  Influences of exogenous probiotics and tea polyphenols on the production of three acids during the simulated colonic fermentation of maize resistant starch..  Journal of food science and technology,  52  ((9)): (5874-5881).  [PMID:26345003]

Solution Calculators